A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639801



Internal ID21831848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151918744..151918859hg38UCSC Ensembl
chrX:151087216..151087331hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103021
Supporting Variants
Samples
Known GenesMAGEA4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639801
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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